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1.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao ; 40(2): 233-241, 2018 Apr 28.
Artigo em Chinês | MEDLINE | ID: mdl-29724314

RESUMO

Objective To evaluate the magnetic resonance imaging (MRI) findings in differential diagnosis between the adult reversible splenial lesion syndrome (RESLES) and ischemic infarction of the splenium of the corpus callosum (SCC). Methods The MRI findings and clinical data of 7 RESLES patients and 13 patients with ischemic infarction of SCC who were clinically diagnosed and treated in our center from May 2015 to June 2017 were analyzed retrospectively. The main MRI findings included location,morphology,signal intensity,maximum cross-sectional area,diffusion weighted imaging (DWI),and apparent diffusion coefficient (ADC) value. Results On the MRI findings of 7 RESLES patients (5 males and 2 females),the centers of all lesions of the SCC were located in the midline of SCC,the lesion shapes were round,ellipse,or spindle,and the distribution of the lesions was bilateral and symmetric as the center of the midline of SCC. The lesions were hyperintense on DWI,and the mean maximum cross-sectional area of lesions was (56.9±32.6) mm2 and the mean ADC value was (0.3963±0.0715) ×10-3 mm2/s. On the review MRI,all the lesions disappeared (mean interval:10 days). On the MRI findings of 13 patients with ischemic infarction of SCC (10 males and 3 females),the lesions were irregular or patchy in shape and were almost laterally and asymmetrically distributed. The lesions were hyperintense on DWI,and the mean maximum cross-sectional area was (55.1±43.9) mm2 and the mean ADC value was (0.4978±0.0123) ×10-3 mm2/s. The mean maximum cross-sectional area (t=0.096,P=0.925) and the ADC value (t=-1.988,P=0.062) were not significantly different between RESLES group and ischemic infarction of SCC group. Conclusions The location,morphology,and distribution of the SCC lesions and the co-existence of other lesions in the brain are helpful for the differential diagnosis between RESLES and ischemic infarction of SCC. However,the mean maximum cross-sectional area and the ADC value show no obvious difference between these two diseases.


Assuntos
Encefalopatias/diagnóstico por imagem , Corpo Caloso/diagnóstico por imagem , Corpo Caloso/patologia , Infarto/diagnóstico por imagem , Imageamento por Ressonância Magnética , Adulto , Diagnóstico Diferencial , Imagem de Difusão por Ressonância Magnética , Feminino , Humanos , Masculino , Estudos Retrospectivos
2.
Curr Drug Targets CNS Neurol Disord ; 4(2): 121-5, 2005 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15857297

RESUMO

This review discusses the potential usefulness of several selected polypeptide growth factors as treatments for stroke. Distinctions between global vs. focal cerebral ischemia, permanent vs. temporary focal ischemia, and acute stroke vs. stroke recovery are first discussed. Potential routes of administration of growth factors are also considered. The growth factors basic fibroblast growth factor (bFGF), osteogenic protein-1 (OP-1), vascular endothelial growth factor (Veg-f), erythropoietin (EPO), and granulocyte colony stimulating factor (G-CSF) all show potential usefulness in animal models of acute stroke and stroke recovery. Two of these factors, bFGF and EPO, have reached human clinical trials for acute stroke, and the data are discussed. Future directions in this field are also discussed.


Assuntos
Isquemia Encefálica/tratamento farmacológico , Eritropoetina/administração & dosagem , Fator 2 de Crescimento de Fibroblastos/administração & dosagem , Acidente Vascular Cerebral/tratamento farmacológico , Animais , Proteína Morfogenética Óssea 7 , Proteínas Morfogenéticas Ósseas/administração & dosagem , Isquemia Encefálica/classificação , Vias de Administração de Medicamentos , Fator Estimulador de Colônias de Granulócitos/administração & dosagem , Substâncias de Crescimento/administração & dosagem , Humanos , Camundongos , Ratos , Acidente Vascular Cerebral/classificação , Fator de Crescimento Transformador beta/administração & dosagem , Fatores de Crescimento do Endotélio Vascular/administração & dosagem
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